<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>5</volume><submitter>Gabriel HB</submitter><pubmed_abstract>Malaria is a tropical disease with significant morbidity and mortality. A better understanding of the metabolism of its most important etiological agent, Plasmodium falciparum, is paramount to the development of better treatment and other mitigation measures. Farnesyldiphosphate synthase/geranylgeranyldiphosphate synthase (FPPS/GGPPS) is a key enzyme in the synthesis of isoprenic chains present in many essential structures. In P. falciparum, as well as a handful of other organisms, FPPS/GGPPS has been shown to be a bifunctional enzyme. By genetic tagging and microscopy, we observed a changing localization of FPPS/GGPPS in blood stage parasites. Given the great importance of alternative splicing and other transcriptional phenomena in gene regulation and the generation of protein diversity, </pubmed_abstract><journal>Scientific reports</journal><pagination>18429</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4685265</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Single-target high-throughput transcription analyses reveal high levels of alternative splicing present in the FPPS/GGPPS from Plasmodium falciparum.</pubmed_title><pmcid>PMC4685265</pmcid><pubmed_authors>Katzin AM</pubmed_authors><pubmed_authors>de Azevedo MF</pubmed_authors><pubmed_authors>Gabriel HB</pubmed_authors><pubmed_authors>Wunderlich G</pubmed_authors><pubmed_authors>Alves JM</pubmed_authors><pubmed_authors>Palmisano G</pubmed_authors><pubmed_authors>Kimura EA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Single-target high-throughput transcription analyses reveal high levels of alternative splicing present in the FPPS/GGPPS from Plasmodium falciparum.</name><description>Malaria is a tropical disease with significant morbidity and mortality. A better understanding of the metabolism of its most important etiological agent, Plasmodium falciparum, is paramount to the development of better treatment and other mitigation measures. Farnesyldiphosphate synthase/geranylgeranyldiphosphate synthase (FPPS/GGPPS) is a key enzyme in the synthesis of isoprenic chains present in many essential structures. In P. falciparum, as well as a handful of other organisms, FPPS/GGPPS has been shown to be a bifunctional enzyme. By genetic tagging and microscopy, we observed a changing localization of FPPS/GGPPS in blood stage parasites. Given the great importance of alternative splicing and other transcriptional phenomena in gene regulation and the generation of protein diversity, </description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Dec</publication><modification>2026-05-05T07:47:53.255Z</modification><creation>2019-03-27T02:05:30Z</creation></dates><accession>S-EPMC4685265</accession><cross_references><pubmed>26688062</pubmed><doi>10.1038/srep18429</doi></cross_references></HashMap>